Variant report

Variant	rs7811688
Chromosome Location	chr7:118740537-118740538
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10229061	0.86[EUR][1000 genomes]
rs10230384	0.86[EUR][1000 genomes]
rs10238286	0.86[EUR][1000 genomes]
rs11974339	0.86[EUR][1000 genomes]
rs12333381	0.94[EUR][1000 genomes]
rs12530696	0.86[EUR][1000 genomes]
rs12535568	0.86[EUR][1000 genomes]
rs17142040	0.90[EUR][1000 genomes]
rs2402472	0.86[EUR][1000 genomes]
rs28409111	0.85[AMR][1000 genomes]
rs2896282	0.86[EUR][1000 genomes]
rs5008597	0.84[EUR][1000 genomes]
rs56015007	0.85[AMR][1000 genomes]
rs58247451	0.89[AMR][1000 genomes]
rs58579703	0.89[AMR][1000 genomes]
rs58825456	0.84[EUR][1000 genomes]
rs58954362	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61262878	0.86[EUR][1000 genomes]
rs6960072	0.86[EUR][1000 genomes]
rs73478887	0.82[AMR][1000 genomes]
rs73478890	0.85[AMR][1000 genomes]
rs73478892	0.85[AMR][1000 genomes]
rs73718376	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73718386	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73718698	0.81[AMR][1000 genomes]
rs73718780	0.82[AMR][1000 genomes]
rs73718786	0.89[AMR][1000 genomes]
rs7782105	0.82[EUR][1000 genomes]
rs7811650	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889098	chr7:118590050-118896639	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv1825159	chr7:118640865-118842361	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv889099	chr7:118709754-118868426	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv528448	chr7:118733415-118744450	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118735400-118740600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:118739200-118743200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr7:118739400-118740800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr7:118739600-118740600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:118739600-118740800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr7:118739800-118740600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr7:118739800-118740800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr7:118739800-118741400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:118740000-118742800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr7:118740200-118740600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:118740200-118740600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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